{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,25]],"date-time":"2026-07-25T02:12:58Z","timestamp":1784945578148,"version":"3.55.0"},"reference-count":13,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2026,1,28]],"date-time":"2026-01-28T00:00:00Z","timestamp":1769558400000},"content-version":"vor","delay-in-days":27,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,1,1]],"date-time":"2026-01-01T00:00:00Z","timestamp":1767225600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Case Reports in Pediatrics"],"published-print":{"date-parts":[[2026,1]]},"abstract":"<jats:p>\n                    We report an 11\u2010year\u2010old Hispanic male with a PPP1R12A gene de novo heterozygous likely pathogenic mutation, p. (Gln13Arg) (CAG&gt;CGG), c.38\n                    <jats:italic>A<\/jats:italic>\n                    \u2009&gt;\u2009\n                    <jats:italic>G<\/jats:italic>\n                    in Exon 1 (NM_002480.2), detected on whole\u2010exome trio sequencing during his short\u2010stature evaluation. His medical history is remarkable for congenital jejunal atresia diagnosed prenatally and repaired surgically shortly after birth. Notably, he lacks genitourinary anomalies, which are frequently described in individuals with PPP1R12A\u2010related urogenital and brain malformation syndrome (UBMS). An endocrine evaluation revealed growth hormone deficiency with an ectopic posterior pituitary gland and an interrupted pituitary stalk. Despite these findings, his neurodevelopment is advanced compared to peers without any concern for intellectual disability. His most recent gastrointestinal and nutritional workup was normal, and he is demonstrating excellent linear growth and response to somatropin therapy. This case broadens the phenotypic spectrum associated with PPP1R12A mutations by highlighting isolated growth hormone deficiency and jejunal atresia in the absence of genitourinary and neurodevelopmental anomalies. We emphasize the importance of multidisciplinary monitoring and an early endocrine referral in patients with PPP1R12A variants presenting with short stature.\n                  <\/jats:p>","DOI":"10.1155\/crpe\/2247764","type":"journal-article","created":{"date-parts":[[2026,1,29]],"date-time":"2026-01-29T06:34:36Z","timestamp":1769668476000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["PPP1R12A Mutation Presenting With Congenital Jejunal Atresia and Short Stature: A Pediatric Endocrinology Case Report"],"prefix":"10.1155","volume":"2026","author":[{"ORCID":"https:\/\/orcid.org\/0009-0000-0913-3385","authenticated-orcid":false,"given":"Rosita","family":"Saul","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0004-9206-5246","authenticated-orcid":false,"given":"Maya","family":"David","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1621-7688","authenticated-orcid":false,"given":"Jordin","family":"Frasch","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pedro A.","family":"Sanchez-Lara","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3928-5221","authenticated-orcid":false,"given":"Bahareh M.","family":"Schweiger","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,1,28]]},"reference":[{"key":"e_1_2_10_1_2","doi-asserted-by":"publisher","DOI":"10.1126\/science.273.5272.245"},{"key":"e_1_2_10_2_2","unstructured":"AlkhunaiziE.andChitayatD. AdamM. P. FeldmanJ. MirzaaG. M. PagonR. A. WallaceS. E. andAmemiyaA. PPP1R12A-Related Urogenital and\/or Brain Malformation Syndrome 2021 GeneReviews."},{"key":"e_1_2_10_3_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2019.12.004"},{"key":"e_1_2_10_4_2","doi-asserted-by":"publisher","DOI":"10.1093\/humrep\/deac239"},{"key":"e_1_2_10_5_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.64217"},{"key":"e_1_2_10_6_2","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0292664"},{"key":"e_1_2_10_7_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.63876"},{"key":"e_1_2_10_8_2","doi-asserted-by":"publisher","DOI":"10.1002\/mgg3.2223"},{"key":"e_1_2_10_9_2","doi-asserted-by":"publisher","DOI":"10.1186\/s12920-024-02009-z"},{"key":"e_1_2_10_10_2","doi-asserted-by":"publisher","DOI":"10.1159\/000452150"},{"key":"e_1_2_10_11_2","doi-asserted-by":"publisher","DOI":"10.1007\/s00247-018-4070-7"},{"key":"e_1_2_10_12_2","doi-asserted-by":"publisher","DOI":"10.1148\/radiology.165.2.3659371"},{"key":"e_1_2_10_13_2","doi-asserted-by":"publisher","DOI":"10.1210\/jcem-73-1-79"}],"container-title":["Case Reports in Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1155\/crpe\/2247764","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/full-xml\/10.1155\/crpe\/2247764","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1155\/crpe\/2247764","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,2,4]],"date-time":"2026-02-04T10:31:32Z","timestamp":1770201092000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1155\/crpe\/2247764"}},"subtitle":[],"editor":[{"given":"Andrea","family":"Scaramuzza","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"editor"}]}],"short-title":[],"issued":{"date-parts":[[2026,1]]},"references-count":13,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2026,1]]}},"alternative-id":["10.1155\/crpe\/2247764"],"URL":"https:\/\/doi.org\/10.1155\/crpe\/2247764","archive":["Portico"],"relation":{},"ISSN":["2090-6803","2090-6811"],"issn-type":[{"value":"2090-6803","type":"print"},{"value":"2090-6811","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,1]]},"assertion":[{"value":"2025-10-07","order":0,"name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2026-01-10","order":2,"name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}},{"value":"2026-01-28","order":3,"name":"published","label":"Published","group":{"name":"publication_history","label":"Publication History"}}],"article-number":"2247764"}}